N/A
N=39
Minimizing Harm From ADEs by Improving Nurse-Physician Communication
Interdisciplinary Communication · Management, Medication Therapy
Bottom Line
View on ClinicalTrials.gov: NCT00574990 ↗Enrolled (actual)
39
Serious AEs
0.0%
Results posted
Jun 2015
Primary outcome: Primary: Incident Rate for Communication Events — 47.6; 34.74; 34.07 mean events per observation — p=0.01
Study Design & Population
- Study type
- Observational
- Phase
- N/A
- Interventions
- —
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- US Department of Veterans Affairs
- Primary completion
- Sep 2009
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Incident Rate for Communication Events |
47.6; 34.74; 34.07 | 0.01 sig |
| SECONDARY Overall Involvement in Conversation by Roles |
31; 21; 58; 12; 23; 9 | — |
Summary
The purpose of this research study is to examine the clinical processes of care involved with the sharing and communicating of medication management information in the inpatient setting between nurses, pharmacists and physicians. The study is unique in that few studies have examined communication content and processes in depth and in relation to specific clinical care. The study will be conducted in two phases. The first phase involves using three focus groups across three sites (a total of nine) each involving between 6-8 individuals to examine perceptions regarding role and procedures associated with medication management. The focus group discussions will be tape-recorded and analyzed using qualitative methods. The information gleaned will assist us in identifying patterns of problems in enhancing the sharing of information, to develop better measures for assessing communication as well as designing effective interventions to enhance communication.
In the second phase of the study, 400 2-4 hour time slots will be randomly selected over about a 5-week period for nursing staff and 500 events over a 6-week period for physicians to conduct ethnographic observations during which specific communication events will be recorded and coded. Every effort will be made to minimize interruptions during clinical care. This research has not been done in terms of medication management content in the inpatient setting (non-ICU).
Eligibility Criteria
Inclusion Criteria
Providers who are working in the VA on the inpatient setting, including pharmacists, nurses, and physicians.
Exclusion Criteria
Staff who have worked at the VA less than 1 year.
Data sourced from ClinicalTrials.gov (NCT00574990). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.